Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:43955303-43955566 | Common:3; Rare:80 | ||||
chr22:44024185-44024329 | Common:1; Rare:52 | ||||
chr22:45163792-45164014 | Common:2; Rare:79 | ||||
chr22:46250268-46250408 | Common:1; Rare:45 | ||||
chr22:46335601-46335759 | Common:2; Rare:68; Clinvar:7; Clinvar (benign):6 | ||||
chr22:46762526-46762669 | Common:3; Rare:48 | ||||
chr22:50185678-50185940 | Common:5; Rare:105 | ||||
chr22:50628078-50628270 | Common:8; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
chr22:50783623-50783859 | Common:1; Rare:70 | ||||
chr3:3126796-3126984 | Common:4; Rare:76; Clinvar (benign):1 | ||||
chr3:4303253-4303373 | Common:1; Rare:41 | ||||
chr3:4493176-4493350 | Rare:62 | ||||
chr3:8501653-8501854 | Rare:69 | ||||
chr3:9362978-9363109 | Common:1; Rare:50 | ||||
chr3:9792398-9792570 | Rare:47 |